Composition Of Secondary Organic Aerosol Research Articles

Modeling the Size Distribution and Chemical Composition of Secondary Organic Aerosols during the Reactive Uptake of Isoprene-Derived Epoxydiols under Low-Humidity Condition

Modeling the Size Distribution and Chemical Composition of Secondary Organic Aerosols during the Reactive Uptake of Isoprene-Derived Epoxydiols under Low-Humidity Condition

Exploring the composition and volatility of secondary organic aerosols in mixed anthropogenic and biogenic precursor systems

Abstract. Secondary organic aerosol (SOA) formation from mixtures of volatile precursors may be influenced by the molecular interactions of the components of the mixture. Here, we report measurements of the volatility distribution of SOA formed from the photo-oxidation of o-cresol, α-pinene, and their mixtures, representative anthropogenic and biogenic precursors, in an atmospheric simulation chamber. The combination of two independent thermal techniques (thermal denuder, TD, and the Filter Inlet for Gases and Aerosols coupled to a high-resolution time-of-flight chemical ionization mass spectrometer, FIGAERO-CIMS) to measure the particle volatility, along with detailed gas- and particle-phase composition measurements, provides links between the chemical composition of the mixture and the resultant SOA particle volatility. The SOA particle volatility obtained by the two independent techniques showed substantial discrepancies. The particle volatility obtained by the TD was wider, spanning across the LVOC and SVOC range, while the respective FIGAERO-CIMS derived using two different methods (i.e. calibrated Tmax and partitioning calculations) was substantially higher (mainly in the SVOC and IVOC, respectively) and narrow. Although the quantification of the SOA particle volatility was challenging, both techniques and methods showed similar trends, with the volatility of the SOA formed from the photo-oxidation of α-pinene being higher than that measured in the o-cresol system, while the volatility of the SOA particles of the mixture was between those measured at the single-precursor systems. This behaviour could be explained by two opposite effects, the scavenging of the larger molecules with lower volatility produced in the single-precursor experiments that led to an increase in the average volatility and the formation of unique-to-the-mixture products that had higher O:C, MW, OSc‾ and, consequently, lower volatility compared to those derived from the individual precursors. We further discuss the potential limitations of FIGAERO-CIMS to report quantitative volatilities and their implications for the reported results, and we show that the particle volatility changes can be qualitatively assessed, while caution should be taken when linking the chemical composition to the particle volatility. These results present the first detailed observations of SOA particle volatility and composition in mixed anthropogenic and biogenic systems and provide an analytical context that can be used to explore particle volatility in chamber experiments.

Phase state of secondary organic aerosol in chamber photo-oxidation of mixed precursors

Abstract. The phase behaviour of aerosol particles plays a profound role in atmospheric physicochemical processes, influencing their physical and optical properties and further impacting climate and air quality. However, understanding of the aerosol phase state is still incomplete, especially that of multicomponent particles which contain inorganic compounds and secondary organic aerosol (SOA) from mixed volatile organic compound (VOC) precursors. We report measurements conducted in the Manchester Aerosol Chamber (MAC) to investigate the aerosol rebounding tendency, measured as the bounce fraction, as a surrogate of the aerosol phase state during SOA formation from photo-oxidation of biogenic (α-pinene and isoprene) and anthropogenic (o-cresol) VOCs and their binary mixtures on deliquescent ammonium sulfate seed. Aerosol phase state is dependent on relative humidity (RH) and chemical composition (key factors determining aerosol water uptake). Liquid (bounce fraction; BF < 0.2) at RH > 80 % and nonliquid behaviour (BF > 0.8) at RH < 30 % were observed, with a liquid-to-nonliquid transition with decreasing RH between 30 % and 80 %. This RH-dependent phase behaviour (RHBF=0.2,0.5,0.8) increased towards a maximum, with an increasing organic–inorganic mass ratio (MRorg/inorg) during SOA formation evolution in all investigated VOC systems. With the use of comparable initial ammonium sulfate seed concentration, the SOA production rate of the VOC systems determines the MRorg/inorg and, consequently, the change in the phase behaviour. Although less important than RH and MRorg/inorg, the SOA composition plays a second-order role, with differences in the liquid-to-nonliquid transition at moderate MRorg/inorg of ∼1 observed between biogenic-only (anthropogenic-free) and anthropogenic-containing VOC systems. Considering the combining role of the RH and chemical composition in aerosol phase state, the BF decreased monotonically with increasing hygroscopic growth factor (GF), and the BF was ∼0 when GF was larger than 1.15. The real atmospheric consequences of our results are that any processes changing ambient RH or MRorg/inorg (aerosol liquid water) will influence their phase state. Where abundant anthropogenic VOCs contribute to SOA, compositional changes in SOA may influence phase behaviour at moderate organic mass fraction (∼50 %) compared with purely biogenic SOA. Further studies are needed on more complex and realistic atmospheric mixtures.

Photodegradation of α-Pinene Secondary Organic Aerosol Dominated by Moderately Oxidized Molecules.

Atmospheric secondary organic aerosol (SOA) undergoes chemical and physical changes when exposed to UV radiation, affecting the atmospheric lifetime of the involved molecules. However, these photolytic processes remain poorly constrained. Here, we present a study aimed at characterizing, at a molecular level and in real time, the chemical composition of α-pinene SOA exposed to UV-A light at 50% relative humidity in an atmospheric simulation chamber. Significant SOA mass loss is observed at high loadings (∼100 μg m-3), whereas the effect is less prevalent at lower loadings (∼20 μg m-3). For the vast majority of molecules measured by the extractive electrospray time-of-flight mass spectrometer, there is a fraction that is photoactive and decays when exposed to UV-A radiation and a fraction that appears photorecalcitrant. The molecules that are most photoactive contain between 4 and 6 oxygen atoms, while the more highly oxygenated compounds and dimers do not exhibit significant decay. Overall, photolysis results in a reduction of the volatility of SOA, which cannot be explained by simple evaporative losses but requires either a change in volatility related to changes in functional groups or a change in physical parameters (i.e., viscosity).

Comparison of methods of functional group analysis using results from laboratory and field aerosol measurements

A study was conducted to compare two methods for analysis of functional groups in secondary organic aerosol (SOA) generated in the laboratory and organic aerosol collected in the Southeastern Oxidants and Aerosol Study (SOAS). Although not as widely used as molecular and elemental analysis, functional group analysis of filter samples provides chemically specific information that can be used to characterize organic aerosol sources, mechanisms of formation, and physical-chemical properties. Here, we compared measurements made using Fourier Transform Infrared (FTIR) spectroscopy, the most widely used method of functional group analysis, with those made using derivatization-spectrophotometric methods. When used to analyze SOA generated from a series of environmental chamber reactions, the methods agreed quite well when results were assigned to four groups: (1) functional groups that contain an O–H bond; (2) non-acid functional groups containing a C = O moiety; (3) organonitrate groups; and (4) alkane groups. Overall, the agreement between the two methods indicates that either is adequate for measuring the functional group composition of SOA. While the derivitization-spectrophotometric methods offer more specificity, they also require more time and aerosol mass for sample analysis than the FTIR methods. It was also shown that functional group signatures obtained from SOA generated in environmental chambers can potentially be used to gain insight into oxidation and particle-phase reactions responsible for SOA formation in field samples.Copyright © 2021 American Association for Aerosol Research

Characterization of secondary organic aerosol from heated-cooking-oil emissions: evolution in composition and volatility

Abstract. Cooking emissions account for a major fraction of urban organic aerosol. It is therefore important to understand the atmospheric evolution in the physical and chemical properties of organic compounds emitted from cooking activities. In this work, we investigate the formation of secondary organic aerosol (SOA) from oxidation of gas-phase organic compounds from heated cooking oil. The chemical composition of cooking SOA is analyzed using thermal desorption–gas chromatography–mass spectrometry (TD–GC–MS). While the particle-phase composition of SOA is a highly complex mixture, we adopt a new method to achieve molecular speciation of the SOA. All the GC-elutable material is classified by the constituent functional groups, allowing us to provide a molecular description of its chemical evolution upon oxidative aging. Our results demonstrate an increase in average oxidation state (from −0.6 to −0.24) and decrease in average carbon number (from 5.2 to 4.9) with increasing photochemical aging of cooking oil, suggesting that fragmentation reactions are key processes in the oxidative aging of cooking emissions within 2 d equivalent of ambient oxidant exposure. Moreover, we estimate that aldehyde precursors from cooking emissions account for a majority of the SOA formation and oxidation products. Overall, our results provide insights into the atmospheric evolution of cooking SOA, a majority of which is derived from gas-phase oxidation of aldehydes.

Anthropogenic Effects on Biogenic Secondary Organic Aerosol Formation

Anthropogenic emissions alter biogenic secondary organic aerosol (SOA) formation from naturally emitted volatile organic compounds (BVOCs). We review the major laboratory and field findings with regard to effects of anthropogenic pollutants (NOx, anthropogenic aerosols, SO2, NH3) on biogenic SOA formation. NOx participate in BVOC oxidation through changing the radical chemistry and oxidation capacity, leading to a complex SOA composition and yield sensitivity towards NOx level for different or even specific hydrocarbon precursors. Anthropogenic aerosols act as an important intermedium for gas—particle partitioning and particle-phase reactions, processes of which are influenced by the particle phase state, acidity, water content and thus associated with biogenic SOA mass accumulation. SO2 modifies biogenic SOA formation mainly through sulfuric acid formation and accompanies new particle formation and acid-catalyzed heterogeneous reactions. Some new SO2-involved mechanisms for organosulfate formation have also been proposed. NH3/amines, as the most prevalent base species in the atmosphere, influence biogenic SOA composition and modify the optical properties of SOA. The response of SOA formation behavior to these anthropogenic pollutants varies among different BVOCs precursors. Investigations on anthropogenic—biogenic interactions in some areas of China that are simultaneously influenced by anthropogenic and biogenic emissions are summarized. Based on this review, some recommendations are made for a more accurate assessment of controllable biogenic SOA formation and its contribution to the total SOA budget. This study also highlights the importance of controlling anthropogenic pollutant emissions with effective pollutant mitigation policies to reduce regional and global biogenic SOA formation.

Effect of relative humidity on SOA formation from aromatic hydrocarbons: Implications from the evolution of gas- and particle-phase species

Relative humidity (RH) plays a significant role in secondary organic aerosol (SOA) formation, but the mechanisms remain uncertain. Using a 30 m3 indoor smog chamber, the influences of RH on SOA formation from two conventional anthropogenic aromatics (toluene and m-xylene) were investigated from the perspective of both the gas- and particle- phases based on the analysis of multi-generation gas-phase products and the chemical composition of SOA, which clearly distinguishes from many previous works mainly focused on the particle-phase. Compared to experiments with RH of 2.0%, SOA yields increased by 11.1%–133.4% and 4.0%–64.5% with higher RH (30.0%–90.0%) for toluene and m-xylene, respectively. The maximum SOA concentration always appeared at 50.0% RH, which is consistent with the change trend of SOA concentration with RH in the summertime field observation. The most plausible reason is that the highest gas-phase OH concentration was observed at 50.0% RH, when the increases in gas-phase OH formation and OH uptake to aerosols and chamber walls with increasing RH reached a balance. The maximum OH concentration was accompanied by a notable decay of second-generation products and formation of third-generation products at 50.0% RH. With further increasing RH, more second-generation products with insufficient oxidation degree will be partitioned into the aerosol phase, and the aqueous-phase oxidation process will also be promoted due to the enhanced uptake of OH. These processes concurrently caused the O/C and oxidation state of carbon (OSc) to first increase and then slightly decrease. This work revealed the complex influence of RH on SOA formation from aromatic VOCs through affecting the OH concentration, partitioning of advanced gas-phase oxidation products as well as aqueous-phase oxidation processes. Quantitative studies to elucidate the role of RH in the partitioning of oxidation products should be conducted to further clarify the mechanism of the influence of RH on SOA formation.

Particle Size Distribution Dynamics Can Help Constrain the Phase State of Secondary Organic Aerosol.

Particle phase state is a property of atmospheric aerosols that has important implications for the formation, evolution, and gas/particle partitioning of secondary organic aerosol (SOA). In this work, we use a size-resolved chemistry and microphysics model (Statistical Oxidation Model coupled to the TwO Moment Aerosol Sectional (SOM-TOMAS)), updated to include an explicit treatment of particle phase state, to constrain the bulk diffusion coefficient (Db) of SOA produced from α-pinene ozonolysis. By leveraging data from laboratory experiments performed in the absence of a seed and under dry conditions, we find that the Db for SOA can be constrained ((1-7) × 10-15 cm2 s-1 in these experiments) by simultaneously reproducing the time-varying SOA mass concentrations and the evolution of the particle size distribution. Another version of our model that used the predicted SOA composition to calculate the glass-transition temperature, viscosity, and, ultimately, Db (∼10-15 cm2 s-1) of the SOA was able to reproduce the mass and size distribution measurements when we included oligomer formation (oligomers accounted for about a fifth of the SOA mass). Our work highlights the potential of a size-resolved SOA model to constrain the particle phase state of SOA using historical measurements of the evolution of the particle size distribution.

Low molecular weight dicarboxylic acids, oxocarboxylic acids and α-dicarbonyls as ozonolysis products of isoprene: Implication for the gaseous-phase formation of secondary organic aerosols

Oxidation of isoprene, a major biogenic volatile organic compound emitted from forest canopies, is a potential source of oxalic acid; the dominant species in organic aerosols. We evaluated here ozonolysis of isoprene in dry darkness as a source of oxalic (C2), malonic (C3) and succinic (C4) acids. We found that oxalic acid and methylglyoxal are dominant products within 10 min of reaction followed by glyoxylic, malonic or succinic acids. Interestingly, molecular distributions of oxidation products from early reactions (9–29 min) were characterized by the predominance of methylglyoxal followed by C2, which became dominant after 30 min. The isoprene-derived secondary organic aerosols (SOAs) showed chemical evolution with reaction time towards the molecular characteristics of dicarboxylic acids similar to those of ambient aerosols (C2>C3≥C4). The carbon-based relative abundances of methylglyoxal decreased steadily (40%→30%), while those of C2 increased with reaction time (15%→25%), but no such variations persisted for glyoxal (6–10%). This finding means that methylglyoxal is more important intermediate of oxalic acid than glyoxal. In contrast, smaller variability and lower concentrations of pyruvic and glyoxylic acids than other intermediates indicate that oxalic acid formation under dry conditions follows a different pathway than in aqueous-phase heterogeneous chemistry usually invoked for cloud/fog/atmospheric waters. Here, we propose new reaction schemes for high levels of methylglyoxal and oxalic acid via gas-phase chemical reactions with ozone and OH radicals to better interpret the ambient SOA composition. Furthermore, the relative abundances of C2 exhibit small variability from 1 to 8 h, suggesting its stable character towards the oxidation by hydroxyl radicals.

Kinetic modeling of formation and evaporation of secondary organic aerosol from NO<sub>3</sub> oxidation of pure and mixed monoterpenes

Abstract. Organic aerosol constitutes a major fraction of the global aerosol burden and is predominantly formed as secondary organic aerosol (SOA). Environmental chambers have been used extensively to study aerosol formation and evolution under controlled conditions similar to the atmosphere, but quantitative prediction of the outcome of these experiments is generally not achieved, which signifies our lack in understanding of these results and limits their portability to large-scale models. In general, kinetic models employing state-of-the-art explicit chemical mechanisms fail to describe the mass concentration and composition of SOA obtained from chamber experiments. Specifically, chemical reactions including the nitrate radical (NO3) are a source of major uncertainty for assessing the chemical and physical properties of oxidation products. Here, we introduce a kinetic model that treats gas-phase chemistry, gas–particle partitioning, particle-phase oligomerization, and chamber vapor wall loss and use it to describe the oxidation of the monoterpenes α-pinene and limonene with NO3. The model can reproduce aerosol mass and nitration degrees in experiments using either pure precursors or their mixtures and infers volatility distributions of products, branching ratios of reactive intermediates and particle-phase reaction rates. The gas-phase chemistry in the model is based on the Master Chemical Mechanism (MCM) but trades speciation of single compounds for the overall ability of quantitatively describing SOA formation by using a lumped chemical mechanism. The complex branching into a multitude of individual products in MCM is replaced in this model with product volatility distributions and detailed peroxy (RO2) and alkoxy (RO) radical chemistry as well as amended by a particle-phase oligomerization scheme. The kinetic parameters obtained in this study are constrained by a set of SOA formation and evaporation experiments conducted in the Georgia Tech Environmental Chamber (GTEC) facility. For both precursors, we present volatility distributions of nitrated and non-nitrated reaction products that are obtained by fitting the kinetic model systematically to the experimental data using a global optimization method, the Monte Carlo genetic algorithm (MCGA). The results presented here provide new mechanistic insight into the processes leading to formation and evaporation of SOA. Most notably, the model suggests that the observed slow evaporation of SOA could be due to reversible oligomerization reactions in the particle phase. However, the observed non-linear behavior of precursor mixtures points towards a complex interplay of reversible oligomerization and kinetic limitations of mass transport in the particle phase, which is explored in a model sensitivity study. The methodologies described in this work provide a basis for quantitative analysis of multi-source data from environmental chamber experiments but also show that a large data pool is needed to fully resolve uncertainties in model parameters.

Simulation of secondary organic aerosol over the Yangtze River Delta region: The impacts from the emissions of intermediate volatility organic compounds and the SOA modeling framework

Secondary organic aerosols (SOA) are an important component of fine particulate matter (PM2.5). However, photochemical models often have difficulty capturing the observed magnitudes of SOA due to uncertainties in precursor emissions and modeling approach. In this study, we conducted a modeling study of SOA in the Yangtze River Delta (YRD) region of China to investigate the impact of emissions of intermediate-volatility organic compounds (IVOC) and the SOA modeling schemes. IVOC emissions, which are important SOA precursors but are missing from most emission inventories, are estimated for the YRD region based on two methods. First, scaling IVOC from emissions of primary organic aerosols (POA) estimates 730 Gg with on-road and industry sectors being the main contributors. Second, scaling IVOC emissions using emission factors and activity data estimates 313 Gg, 57% lower than the first method, with industry and off-road sectors being the major contributors. A photochemical model simulation of SOA for July 2018, conducted using standard emission inventories for the YRD region, significantly underestimates SOA by 61% at the Dianshan Lake monitoring site (DSL). A series of simulations with two different SOA modeling schemes found that with the traditional two-product modeling framework, IVOC emissions enhance simulated SOA concentrations by 8%–27% at DSL and 5%–26% over the YRD region in July 2018. Increasing SOA mass yields from IVOC by a factor of five leads to better agreement with observations at the DSL site. Switching to the 1.5-Dimension Volatility Basis Set (VBS) approach increases simulated SOA by 76% at DSL but reduced POA concentration by 72%, leading to an overall decrease of organic aerosol (OA) by 12%. Unlike the two-product scheme where POA is entirely inert, the VBS scheme includes POA in the OA chemistry. The SOA:OA ratio and the anthropogenic-to-biogenic SOA ratio (ASOA:BSOA) also vary systematically with SOA modeling schemes suggesting that detailed measurements of SOA composition could further constrain modeling methods.

Relative contributions of selected multigeneration products to chamber SOA formed from photooxidation of a range (C10–C17) of n-alkanes under high NOx conditions

A series of chamber experiments was conducted to investigate the composition of secondary organic aerosol (SOA) following oxidation of a range of parent n-alkanes (C10–C17) in the presence of NOx. The relative contribution of selected species representing first, second, and higher generation products to SOA mass was measured using a high-resolution aerosol mass spectrometer. Gas chromatography was also used for a limited set of amenable species. Relative contributions varied substantially across the range of investigated alkanes reflecting slight changes in SOA composition. The contribution of first-generation cyclic hemiacetal is minimal toward the small end of the investigated range and gradually increases with n-alkane size. The relative contributions of second generation and higher nitrate-containing species, in contrast, decrease with an increased alkane size. A similar trend is observed for relative contribution of organonitrates to SOA. Finally, SOA yield and composition are sensitive to water vapor concentrations. This sensitivity is limited to a narrow range (dry to ~15% RH) with little, if any, impact above 15% suggesting that this impact may be negligible under ambient conditions. The impact of water vapor also appears to decrease with increasing alkane carbon number.

Indoor secondary organic aerosols: Towards an improved representation of their formation and composition in models.

The formation of secondary organic aerosol (SOA) indoors is one of the many consequences of the rich and complex chemistry that occurs therein. Given particulate matter has well documented health effects, we need to understand the mechanism for SOA formation indoors and its resulting composition. This study evaluates some uncertainties that exist in quantifying gas-to-particle partitioning of SOA-forming compounds using an indoor detailed chemical model. In particular, we investigate the impacts of using different methods to estimate compound vapour pressures as well as simulating the formation of highly oxygenated organic molecules (HOM) via auto-oxidation on SOA formation indoors. Estimation of vapour pressures for 136 α-pinene oxidation species by six investigated methods led to standard deviations of 28-216%. Inclusion of HOM formation improved model performance across three of the six assessed vapour pressure estimation methods when comparing against experimental data, particularly when the NO2 concentration was relatively high. We also explored the predicted SOA composition using two product classification methods, the first assuming the molecule is dominated by one functionality according to its name, and the second accounting for the fractional weighting of each functional group within a molecule. The SOA composition was dominated by the HOM species when the NO2-to-α-terpineol ratio was high for both product classification methods, as these conditions promoted formation of the nitrate radical and hence formation of HOM monomers. As the NO2-to-α-terpineol ratio decreased, peroxides and acids dominated the simple classification, whereas for the fractional classification, carbonyl and alcohol groups became more important.

Temperature effects on optical properties and chemical composition of secondary organic aerosol derived from <i>n</i>-dodecane

Abstract. Environmental temperature plays a vital role in controlling chemical transformations that lead to the formation of secondary organic aerosol (SOA) and ultimately impact the composition and optical properties of the aerosol particles. In this study, we investigated optical properties of n-dodecane SOA under two temperature conditions: 5 and 25 ∘C. It was shown that low-temperature conditions could enhance the real part of the refractive index (RI) of the SOA at wavelengths of 532 and 375 nm. Mass spectrometry analysis revealed that the molecular composition of n-dodecane SOA was significantly modified by temperature: a large amount of oligomers were formed under low-temperature conditions, which led to higher RI values. These findings will help improve our understanding of the chemical composition and optical properties of SOA under different temperature conditions and will provide one possible explanation for the low visibility in suburban areas during winter.

Coupling Filter-Based Thermal Desorption Chemical Ionization Mass Spectrometry with Liquid Chromatography/Electrospray Ionization Mass Spectrometry for Molecular Analysis of Secondary Organic Aerosol.

Filter-based thermal desorption (F-TD) techniques, such as the filter inlet for gases and aerosols, are widely employed to investigate the molecular composition and physicochemical properties of secondary organic aerosol (SOA). Here, we introduce an enhanced capability of F-TD through the combination of a customized F-TD inlet with chemical ionization mass spectrometry (CIMS) and ultraperformance liquid chromatography/electrospray ionization mass spectrometry (UPLC/ESI-MS). The utility of F-TD/CIMS + UPLC/ESI-MS is demonstrated by application to α-pinene ozonolysis SOA for which increased filter aerosol mass loading is shown to slow the evaporation rates of deposited compounds. Evidence for oligomer decomposition producing multimode F-TD/CIMS thermograms is provided by the measurement of the mass fraction remaining of monomeric and dimeric α-pinene oxidation products on the filter via UPLC/ESI-MS. In situ evaporation of aerosol particles suggests that α-pinene-derived hydroperoxides are thermally labile; thus, analysis of particle-phase (hydro)peroxides via F-TD may not be appropriate. A synthesized pinene-derived dimer ester (C20H32O5) is found to be thermally stable up to 200 °C, whereas particle-phase dimers (C19H30O5) are observed to form during F-TD analysis via thermally induced condensation of synthesized pinene-derived alcohols and diacids. The complementary F-TD/CIMS + UPLC/ESI-MS method offers previously inaccessible insight into the molecular composition and thermal desorption behavior of SOA that both clarifies and expands on analysis via traditional F-TD techniques.

Effect of the nitrate group on yields and composition of secondary organic aerosol formed from reactions of alkyl nitrates with OH radicals in the presence of NOx

A systematic study was conducted on the effect of a nitrate functional group on secondary organic aerosol (SOA) products and yields from reactions of C10 alkyl nitrate isomers with OH radicals in the presence of NOx. The 1- through 5-decyl nitrate isomers were synthesized from their corresponding alcohols, reacted in an environmental chamber, and the precursors and SOA were analyzed using online and offline techniques. SOA products were analogous to those formed from similar reactions of the C10 n-alkane (decane), but with an additional nitrate group. The SOA yield was highest when the nitrate group was on the terminal carbon and decreased monotonically from 0.51 to 0.50, 0.44, 0.28, and 0.15 as it moved toward the center of the molecule, at which point it was similar to that from decane. The explanation for this trend, which is supported by results of calculations performed using a kinetics model, involves a combination of the effects of the nitrate group on product vapor pressures and reaction branching ratios. In general, although the nitrate group lowers the vapor pressures of products relative to the corresponding products of the decane reaction, thus enhancing gas-to-particle partitioning and SOA formation, as it moves toward the center of the molecule it also alters the branching ratios for reaction pathways so as to enhance the formation of more volatile products. The results are compared with those from similar studies on ketone and alcohol isomers to gain a more comprehensive understanding of the effects of functional groups on SOA composition and yields.Copyright © 2020 American Association for Aerosol Research

Effects of NOx and SO2 on the secondary organic aerosol formation from the photooxidation of 1,3,5-trimethylbenzene: A new source of organosulfates

1,3,5-Trimethylbeneze (TMB) is an important constituent of anthropogenic volatile organic compounds that contributes to the formation of secondary organic aerosol (SOA). A series of chamber experiments were performed to probe the effects of NOx and SO2 on SOA formation from TMB photooxidation. The molecular composition of TMB SOA was investigated by ultra-high performance liquid chromatography/electrospray ionization high-resolution quadrupole time-of-flight mass spectrometry (UPLC/ESI-HR-Q-TOFMS). We found that the SOA yield increases notably with elevated NOx concentrations under low-NOx condition ([TMB]0/[NOx]0 > 10 ppbC ppb−1), while an opposite trend is observed in high-NOx experiments ([TMB]0/[NOx]0 < 10 ppbC ppb−1). The increase in SOA yield in low-NOx regime is attributed to the increase of NOx-induced OH concentrations. The formation of low-volatility species might be suppressed, thereby leading to a lower SOA yield in high-NOx conditions. Moreover, SOA formation was promoted in experiment with SO2 addition. Multifunctional products containing carbonyl, acid, alcohol, and nitrate functional groups were characterized in TMB/NOx photooxidation, whereas several organosulfates (OSs) and nitrooxy organosulfates were identified in TMB/NOx/SO2 photooxidation based on HR-Q-TOFMS analysis. The formation mechanism relevant to the detected compounds in SOA were proposed. Based on our measurements, the photooxidation of TMB in the presence of SO2 may be a new source of OSs in the atmosphere. The results presented here also deepen the understanding of SOA formation under relatively complex polluted environments.

Effects of SO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; on optical properties of secondary organic aerosol generated from photooxidation of toluene under different relative humidity conditions

Abstract. Secondary organic aerosol (SOA) has great impacts on air quality, climate change and human health. The composition and physicochemical properties of SOA differ greatly because they form under different atmospheric conditions and from various precursors as well as differing oxidation. In this work, photooxidation experiments of toluene were performed under four conditions (dry, dry with SO2, wet and wet with SO2) to investigate the effect of SO2 under different relative humidities on the composition and optical properties of SOA at wavelengths of 375 and 532 nm. According to our results, the increase in humidity enhances not only light absorption but also the scattering property of the SOA. Oligomers formed through multiphase reactions might be the reason for this phenomenon. Adding SO2 slightly lowers the real part of the complex refractive index, RI(n), of toluene-derived SOA (RI(n)dry,SO2&lt;RI(n)dry, RI(n)wet,SO2&lt;RI(n)wet), which might be a result of the partitioning of low-oxidation-state products. The imaginary part of the complex refractive index, RI(k), is enhanced under dry conditions with SO2 compared to that of only dry conditions, which might be due to acid-catalyzed aldol condensation reactions. Wet conditions with SO2 shows the combined effect of SO2 and humidity. The extinction properties of toluene-derived SOA under wet conditions with SO2 increased by approximately 30 % compared to that of toluene-derived SOA formed under dry conditions. Our results suggest that various atmospheric conditions will affect the composition and optical proprieties of SOA, which has significant implications for evaluating the impacts of SOA on the rapid formation of regional haze, global radiative balance and climate change.

Exploring the formation potential and optical properties of secondary organic aerosol from the photooxidation of selected short aliphatic ethers

Secondary organic aerosol (SOA) formation potential for six kinds of short aliphatic ethers has been studied. The size distribution, mass concentration, and yield of SOA formed by ethers photooxidation were determined under different conditions. The results showed that all six ethers can generate SOA via reaction with OH radicals even under no seed and NOx-free condition. The mass concentration for six seedless experiments was less than 10 µg/m3 and the SOA yields were all below 1%. The strong increase in the SOA formation was observed when the system contained ammonium sulfate seed particles, while SOA yield decreased under the high-NOx condition. SOA composition was analyzed using offline methods. Infrared spectra indicated that there are complex components in the particle-phase including carbonyls acid and aldehydes species. Moreover, the aqueous filter extracts were analyzed using ultraviolet-visible spectrometer and fluorescence spectrophotometer. For the fresh methyl n-butyl ether SOA, the largest absorption peak occurs at 280 nm and there exists slightly absorption in the 300–400 nm. Excitation-emission matrices display the distinct peak at excitation/emission = 470 nm/480 nm according to the fluorescence spectrum. These findings are important considerations of formation for ether SOA that can eventually be included in atmospheric models.